1yjv

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[[Image:1yjv.gif|left|200px]]
[[Image:1yjv.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1yjv |SIZE=350|CAPTION= <scene name='initialview01'>1yjv</scene>
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The line below this paragraph, containing "STRUCTURE_1yjv", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=CU1:COPPER+(I)+ION'>CU1</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Copper-exporting_ATPase Copper-exporting ATPase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.6.3.4 3.6.3.4] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE= ATP7A ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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-->
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|DOMAIN=
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{{STRUCTURE_1yjv| PDB=1yjv | SCENE= }}
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|RELATEDENTRY=[[1yju|1YJU]], [[1yjt|1YJT]], [[1yjr|1YJR]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1yjv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1yjv OCA], [http://www.ebi.ac.uk/pdbsum/1yjv PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1yjv RCSB]</span>
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}}
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'''Solution structure of the Cu(I) form of the sixth soluble domain of Menkes protein'''
'''Solution structure of the Cu(I) form of the sixth soluble domain of Menkes protein'''
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[[Category: Rosato, A.]]
[[Category: Rosato, A.]]
[[Category: Wang, S.]]
[[Category: Wang, S.]]
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[[Category: copper(i)]]
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[[Category: Metal homeostasis]]
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[[Category: metal homeostasis]]
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[[Category: Metallochaperone]]
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[[Category: metallochaperone]]
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[[Category: Protein-protein interaction]]
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[[Category: protein-protein interaction]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 16:24:50 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 01:10:02 2008''
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Revision as of 13:24, 3 May 2008

Template:STRUCTURE 1yjv

Solution structure of the Cu(I) form of the sixth soluble domain of Menkes protein


Contents

Overview

Menkes disease is a fatal disease that can be induced by various mutations in the ATP7A gene, leading to unpaired uptake of dietary copper. The ATP7A gene encodes a copper(I)-translocating ATPase. Here the disease-causing A629P mutation, which occurs in the last of the six copper(I)-binding soluble domains of the ATPase (hereafter MNK6), was investigated. To understand why this apparently minor amino acid replacement is pathogenic, the solution structures and dynamics on various time-scales of wild-type and A629P-MNK6 were determined both in the apo- and copper(I)-loaded forms. The interaction in vitro with the physiological ATP7A copper(I)-donor (HAH1) was additionally studied. The A629P mutation makes the protein beta-sheet more solvent accessible, possibly resulting in an enhanced susceptibility of ATP7A to proteolytic cleavage and/or in reduced capability of copper(I)-translocation. A small reduction of the affinity for copper(I) is also observed. Both effects could concur to pathogenicity.

Disease

Known disease associated with this structure: Cutis laxa, neonatal OMIM:[300011], Menkes disease OMIM:[300011], Occipital horn syndrome OMIM:[300011]

About this Structure

1YJV is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

An atomic-level investigation of the disease-causing A629P mutant of the Menkes protein, ATP7A., Banci L, Bertini I, Cantini F, Migliardi M, Rosato A, Wang S, J Mol Biol. 2005 Sep 16;352(2):409-17. PMID:16083905 Page seeded by OCA on Sat May 3 16:24:50 2008

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